Cleidocranial Dysplasia Dysplasia, Cleidocranial; Dysplasia, Osteodental; mariesainton disease This disease entry is based upon medical information available through the http://my.webmd.com/hw/raising_a_family/nord961.asp
Extractions: Cleidocranial dysplasia is a rare skeletal dysplasia characterized by short stature, distinctive facial features and narrow, sloping shoulders caused by defective or absent collarbones (clavicles). Major symptoms may include premature closing of the soft spot on the head (coronal), delayed closure of the space between the bones of the skull (fontanels), narrow and abnormally shaped pelvic and pubic bones and deformations in the chest (thoracic region). Delayed eruption of teeth, moderately short stature, a high arched palate, a wide pelvic joint, failure of the lower jaw joints to unite, and fingers that are irregular in length may also be present. Cleidocranial dysplasia is inherited as an autosomal dominant genetic trait.
Birth Disorder Information Directory - M SINDROME DI MARFAN Also see Arachnodactyly Marie Sainton Disease. See Cleidocranial Dysostosis/Dysplasia Marie Strumpell Disease/Spondylitis http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
Definitions Of Genetic Disorders-M. Marie Disease acromeg.htm mariesainton disease cleidocran.htm Marie StrumpellDisease ankspon.htm Marie-Strumpell Spondylitis ankspon.htm http://www.icomm.ca/geneinfo/def-m.htm
Webkatalog Webkatalog des Fit Gesundbereichs http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
Webkatalog Webkatalog f r den Bereich Wissenschaft http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
Entrez PubMed Cleidocranial dysostosis (Pierre mariesainton disease) Article in FrenchMiest D, Malevez C, Putz M. Publication Types Case Reports MeSH Terms http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=1
M - The Health Beat Medical . Disease . Conditions - Marburg@ Marfan Syndrome@ mariesainton disease@ Marinesco-Sjogren Syndrome@ Mayer Rokitansky Kuster Hauser Syndrome@ McArdle's Disease@ http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
Entrez PubMed Apropos of a recent case of Pierre mariesainton disease Article in FrenchTARDOS R, IMBERT JP, LE MARCHAND G. PMID 13775314 PubMed - OLDMEDLINE for http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=1
Definitions Of Genetic Disorders-M. htm Marie's Ataxia marieat.htm Marie Disease acromeg.htm mariesainton disease cleidocran.htm Marie Strumpell Disease ankspon.htm Marie http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
Extractions: It is possible that the main title of the report Cleidocranial Dysplasia is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Cleidocranial dysplasia is a rare skeletal dysplasia characterized by short stature, distinctive facial features and narrow, sloping shoulders caused by defective or absent collarbones (clavicles). Major symptoms may include premature closing of the soft spot on the head (coronal), delayed closure of the space between the bones of the skull (fontanels), narrow and abnormally shaped pelvic and pubic bones and deformations in the chest (thoracic region). Delayed eruption of teeth, moderately short stature, a high arched palate, a wide pelvic joint, failure of the lower jaw joints to unite, and fingers that are irregular in length may also be present. Cleidocranial dysplasia is inherited as an autosomal dominant genetic trait. Children's Craniofacial Association
Health Topics Marfanoid Hypermobility Syndrome, Marie Disease, mariesainton disease, Marine Stingsand Scrapes, Marinesco Sjogren Syndrome, Marinesco-Garland Syndrome, http://www.peacehealth.org/kbase/list/ht/m.htm
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